Clinical Research Associate

ICON Strategic Solutions; France; Hybride; EUR 40 000 - 70 000; Plein temps

Résumé du poste

Join a forward-thinking company as a Clinical Research Associate dedicated to global pharmaceutical clients. In this dynamic role based in Paris, you'll manage investigator sites, ensuring excellence in clinical trials. With a focus on Oncology and Hematology, you'll leverage your expertise to foster relationships and uphold the integrity of clinical data. This position offers the chance to work in a collaborative environment that values innovation and flexibility, making a real impact on life-improving drug development. If you're ready to take your career to the next level, this opportunity is for you.

Qualifications

• Minimum 2-3 years as a CRA in the pharmaceutical industry or CRO.
• Fluency in French and professional proficiency in English.

Responsabilités

• Manage investigator sites for successful study execution.
• Conduct site visits and develop relationships with site staff.
• Ensure integrity of clinical data and maintain tracking records.

Connaissances

Clinical Research

Oncology

Hematology

Site Management

Communication Skills

Organization Skills

IT Skills

Formation

Bachelor's Degree in Life Sciences

Description du poste

We are constantly looking for motivated, reliable and dedicated CRAs who can demonstrate at least 12 months independent external monitoring of commercial studies (or a mix of commercial clinical studies) ideally in Oncology and Hematology. Other therapeutic areas are also of interest, especially if gained on phase I - II or III commercial trials.

As a Clinical Research Associate you will be dedicated to one of our global pharmaceutical clients; with whom ICON shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market. Leading by example, you can set the standard of excellence and enjoy a challenging career in our exclusive programs.

We are currently looking for a Clinical Research Associate to join one of our sponsor-dedicated teams in Paris (2 days ICON office based).

Key responsibilities include:

• Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out
• Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan
• Developing effective relationships with investigator site staff to ensure that key clinical metrics are met
• Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues
• Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines

You will need:

• A first stable experience as a CRA, this within the pharmaceutical industry or a CRO (min 2-3 years)
• Interested in different Therapeutic Areas
• Excellent organization skills
• Ability to work well in a dynamic environment and able to prioritize and respond to changing needs of the business
• Strong IT skills
• Strong communication with the ability to multitask and work effectively under pressure
• Fluency in French and professional proficiency in English

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